Headstart, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Headstart, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SnugKap
1
Total
1
Cleared
0
Denied
Headstart, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Headstart, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Headstart, Ltd.
1 devices